Down syndrome in a population of elderly mentally retarded patients: Genetic-diagnostic survey and implications for medical care

Ninety‐six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic diagnosis, mental functioning and dementia, ophthalmological and audiological abnormalities, and thyroid function. Seventy of the 96 DS patien...

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Published in:American journal of medical genetics Vol. 85; no. 4; pp. 376 - 384
Main Authors: Van Buggenhout, G.J.C.M., Trommelen, J.C.M., Schoenmaker, A., De Bal, C., Verbeek, J.J.M.C., Smeets, D.F.C.M., Ropers, H.H., Devriendt, K., Hamel, B.C.J., Fryns, J.P.
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Abstract Ninety‐six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic diagnosis, mental functioning and dementia, ophthalmological and audiological abnormalities, and thyroid function. Seventy of the 96 DS patients (73%) were older than 40 years. Only 4.2% were females. Trisomy 21 was found in 86% and mosaic trisomy 21 in 13%. Eighty‐two percent of the patients were moderately or severely mentally retarded, 15% were profoundly retarded, and only 3% mildly retarded. Nineteen percent of the patients had dementia. This number increased to 42% of the patients above the age of 50 years. Epileptic seizures were present in 16.7% of all patients, and in 50% of the patients with dementia. Only 17% of the patients in the present study had normal visual acuity, one‐third had at least moderately reduced vision. This number increased significantly with age: in the age group 50–59 years almost half of the patients had moderate to severe vision loss. Seventy percent of the patients had moderate, severe, or very severe hearing loss, which was undiagnosed before systematic hearing testing was performed. Increased (48%) or decreased (1%) TSH level was found in 49% of the patients examined for thyroid functions. We suggest a regular screening of all adults with DS to diagnose early dementia, epilepsy, hypothyroidism, and early loss of visual acuity and hearing, with special attention to the group of patients who are severely to profoundly mentally retarded and those with advanced age. Cytogenetic studies are necessary to confirm the clinical diagnosis and are essential for genetic counseling purposes. Am. J. Med. Genet. 85:376–384, 1999. © 1999 Wiley‐Liss, Inc.
AbstractList Ninety-six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic diagnosis, mental functioning and dementia, ophthalmological and audiological abnormalities, and thyroid function. Seventy of the 96 DS patients (73%) were older than 40 years. Only 4.2% were females. Trisomy 21 was found in 86% and mosaic trisomy 21 in 13%. Eighty-two percent of the patients were moderately or severely mentally retarded, 15% were profoundly retarded, and only 3% mildly retarded. Nineteen percent of the patients had dementia. This number increased to 42% of the patients above the age of 50 years. Epileptic seizures were present in 16.7% of all patients, and in 50% of the patients with dementia. Only 17% of the patients in the present study had normal visual acuity, one-third had at least moderately reduced vision. This number increased significantly with age: in the age group 50-59 years almost half of the patients had moderate to severe vision loss. Seventy percent of the patients had moderate, severe, or very severe hearing loss, which was undiagnosed before systematic hearing testing was performed. Increased (48%) or decreased (1%) TSH level was found in 49% of the patients examined for thyroid functions. We suggest a regular screening of all adults with DS to diagnose early dementia, epilepsy, hypothyroidism, and early loss of visual acuity and hearing, with special attention to the group of patients who are severely to profoundly mentally retarded and those with advanced age. Cytogenetic studies are necessary to confirm the clinical diagnosis and are essential for genetic counseling purposes.
Ninety‐six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic diagnosis, mental functioning and dementia, ophthalmological and audiological abnormalities, and thyroid function. Seventy of the 96 DS patients (73%) were older than 40 years. Only 4.2% were females. Trisomy 21 was found in 86% and mosaic trisomy 21 in 13%. Eighty‐two percent of the patients were moderately or severely mentally retarded, 15% were profoundly retarded, and only 3% mildly retarded. Nineteen percent of the patients had dementia. This number increased to 42% of the patients above the age of 50 years. Epileptic seizures were present in 16.7% of all patients, and in 50% of the patients with dementia. Only 17% of the patients in the present study had normal visual acuity, one‐third had at least moderately reduced vision. This number increased significantly with age: in the age group 50–59 years almost half of the patients had moderate to severe vision loss. Seventy percent of the patients had moderate, severe, or very severe hearing loss, which was undiagnosed before systematic hearing testing was performed. Increased (48%) or decreased (1%) TSH level was found in 49% of the patients examined for thyroid functions. We suggest a regular screening of all adults with DS to diagnose early dementia, epilepsy, hypothyroidism, and early loss of visual acuity and hearing, with special attention to the group of patients who are severely to profoundly mentally retarded and those with advanced age. Cytogenetic studies are necessary to confirm the clinical diagnosis and are essential for genetic counseling purposes. Am. J. Med. Genet. 85:376–384, 1999. © 1999 Wiley‐Liss, Inc.
Author Smeets, D.F.C.M.
Schoenmaker, A.
De Bal, C.
Fryns, J.P.
Devriendt, K.
Verbeek, J.J.M.C.
Trommelen, J.C.M.
Ropers, H.H.
Hamel, B.C.J.
Van Buggenhout, G.J.C.M.
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10.1136/jmg.31.10.807
10.1136/bjo.51.7.469
10.1136/jmg.27.8.505
10.3109/01050399009070760
10.1111/j.1365-2788.1995.tb00909.x
10.1016/S0002-9394(14)76031-3
10.1016/0002-9394(62)93757-1
10.1111/j.1651-2227.1995.tb13768.x
10.12968/bjon.1996.5.10.630
10.1111/j.1755-3768.1988.tb04040.x
10.1001/archinte.1989.00390090058012
10.1192/bjp.155.2.202
10.7326/0003-4819-101-1-18
10.1002/ajmg.1320250124
10.1136/bjo.47.6.321
10.1017/S0033291700024946
10.1093/hmg/4.10.1935
10.1136/bmj.2.5918.533
10.1136/adc.67.5.628
10.1177/000992288902800804
10.1001/archneur.1990.00530030029011
10.1111/j.1365-2788.1992.tb00532.x
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Issue 4
Keywords Chromosomal aberration
Human
Trisomy
Prognosis
Epilepsy
Vision disorder
Chromosome G21
Auditory disorder
Aneuploidy
Down syndrome
Hypothyroidism
Symptomatology
Phenotype
Intellectual deficiency
Genetics
Adult
Complication
Age
Dementia
Language English
License CC BY 4.0
Copyright 1999 Wiley-Liss, Inc.
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References Mattel JF, Mattel MG, Baeteman MA, Giraud F. 1981. Trisomy 21 for the region 21q223: identification by high-resolution R-banding patterns. Hum Genet 56: 409-411.
Mul M, Verhaart W, Bierman A. 1997. Slechthorendheid bij mensen met een verstandelijke handicap in de huisartspraktijk. Huisarts Wet 40: 301-304.
Cullen JF, Butler HG. 1963. Mongolism (Down's syndrome) and keratoconus. Br J Ophthalmol 47: 321-330.
Trommelen J, De Bal C. 1994. Prevalentie van slechthorendheid in een geïnstitutionaliseerde populatie verstandelijk gehandicapten zonder Down syndroom. Logopedie (7) 2: 29-32.
Warburg M. 1982. Why are the blind and severely visually impaired children with mental retardation much more retarded than the sighted children? Acta Ophthalmol Suppl 157: 72-81.
Harper PS. 1994. Practical genetic counseling, 4th rev. ed. Cambridge: Cambridge University Press, p 60-61.
Edwards WC, Price WD, Weisskopf B. 1972. Ocular findings in develop-mentally handicapped children. J Pediatr Ophtalmol 9: 162-167.
Annerén G, Magnusson, CGM, Lilja, G, Nordvall, SL. 1992. Abnormal serum IgG subclass pattern in children with Down's syndrome. Arch Dis Child 62: 628-631.
Evenhuis HM. 1991. Veel voorkomende, maar weinig onderkende aandoeningen bij volwassenen met het syndroom van Down. Ned Tijdschr Geneesk 135: 1581-1584.
Anonymous. 1986. Subclinical hypothyroidism (editorial). Lancet 1: 251-252.
Brown PM, Lewis GTR, Parker AJ, Maw AR. 1989. The skull-base and nasopharynx in Down's syndrome in relation to hearing impairment. Clin Otolaryngol 14: 241-246.
Evenhuis HM, Kengen MMF, Eurlings HAL. 1991. Dementie vragenlijst voor zwakzinnigen (DVZ). Lisse: Swets & Zeitlinger.
Cooper DS, Halpern R, Wood LC, Levin AA, Ridgway EC. 1984. L-thyroxine therapy in subclinical hypothyroidism. Ann Intern Med 101: 18-24.
Crandell CC, Roeser RJ. 1993. Incidence of excessive/impacted cerumen in individuals with mental retardation: a longitudinal investigation. Am J Ment Retard 97: 568-574.
Kinnell HG, Gibbs N, Teale JD, Smith J. 1987. Thyroid dysfunction in institutionalised Down's syndrome adults. Psychol Med 17: 387-392.
Alembik Y, Toledo C, Finck S, Stoll C. 1996. Anomalies of thyroid function in Down syndrome children. Eur J Hum Genet 4 (Suppl 1): 28.
Dahle AJ, McCollister. 1986. Hearing and otologic disorders in children with Down syndrome. Am J Ment Defic 90: 636-642.
Evenhuis HM. 1992. Evaluation of a screening instrument for dementia in ageing mentally retarded persons. J Intellect Disabil Res 36: 337-347.
Dinani S, Carpenter S. 1990. Down's syndrome and thyroid disorder. J Ment Defic Res 34: 187-193.
Pueschel SM, Pezzullo JC. 1985. Thyroid dysfunction in Down syndrome. Am J Dis Child 139: 636-639.
Katz J. 1994. Handbook of clinical audiology, 4th ed. Baltimore: Williams and Wilkins. p 283-285.
Verpoorten RA, Emmen JG. 1995. A tactile-auditory conditioning procedure for the hearing assessment of persons with autism and mental retardation. Scand Audiol 24 (Suppl 41): 49-50.
Stinissen J. 1965. Terman-Merrill Intelligentieschaal-Vorm L-M. Uitgegeven door de Faculteit der Psychologie en Pedagogische Wetenschappen. Katholieke Universiteit Leuven.
Van Haasen PP, Vander Steene G, De Bruyn EEJ et al. 1986. Wechsler intelligence scale for children-revised, Nederlandse uitgave. Lisse: Swets & Zeitlinger.
Buchanan LH. 1990. Early onset of presbyacusis in Down syndrome. Scand Audiol 19: 103-110.
APA (American Psychiatric Association). 1994. Diagnostic and statistical manual of mental disorders, 4th ed. Washington, DC: American Psychiatric Association.
Kraijer DW, Kema GN. 1990. Sociale Redzaamheidsschaal. Lisse: Swets & Zeitlinger.
McGrother CW, Marshall B. 1990. Recent trends in incidence, morbidity and survival in Down's syndrome. J Ment Defic Res 34: 49-57.
Stinissen J, Vander Steene G. 1970. WPPSI: Wechsler preschool and primary scale of intelligence. Handleiding bij de Nederlandse aanpassing. Lisse: Swets & Zeitlinger.
Evenhuis HM, van Zanten GA, Brocaar MP, Roerdinkholder WHM. 1992. Hearing loss in middle-age persons with Down syndrome. Am J Ment Retard 97: 47-56.
Maurizi M, Ottaviani F, Paludetti G. 1995. Objective methods of hearing assessment: an introduction. Scand Audiol 24 (Suppl 41): 5-7.
Thase ME. 1982. Longevity and mortality in Down's syndrome. J Ment Defic Res 26: 177-192.
Van der Meulen BF, Smrkovsky M. 1983. Bayley Scales of Infant Development. Nederlandse Uitgave (BOS 2-30). Lisse: Swets & Zeitlinger.
Eissler R, Longenecker LP. 1962. The common eye findings in mongolism. Am J Ophthalmol 54: 398-406.
Evenhuis HM. 1996. Richtlijnen voor diagnostiek en behandeling van slechthorendheid bij mensen met een verstandelijke handicap. Ned Tijdschr Geneesk 140 (37): 1851-1854.
Kleczkowska A, Fryns JP, Van den Berghe H. 1990. On the variable effect of mosaic normal/balanced chromosomal rearrangements in man. J Med Genet 27: 505-507.
Kelly JS. 1996. Eye examination and vision testing. Br J Nurs 5: 630-634.
Korenberg JR, Kawashima H, Pulst S-M, Ikeuchi T, Ogasawara N, Yama-moto K, Schonberg SA, West R, Allen L, Magenis E, Ikawa K, Tanigu-chi N, Epstein CJ. 1990. Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype. Am J Hum Genet 47: 236-246.
Warren AC, Holroyd S, Folstein MF. 1989. Major depression in Down's syndrome. Br J Psychiatry 155: 202-205.
Fuentes J-J, Pritchard MA, Planas AM, Bosch A, Ferrer I, Estivill X. 1995. A new human gene from the Down syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart. Hum Mol Genet 4: 1935-1944.
Aitchinson C, Easty DL, Jancar J. 1990. Eye abnormalities in the mentally handicapped. J Ment Defic Res 34: 41-48.
Jacobson L. 1988. Ophthalmology in mentally retarded adults. A clinical survey. Acta Ophthalmol 66: 457-462.
Janicki MP, Jacobson JW. 1986. General trends in sensory, physical, and behavioral abilities among older mentally retarded persons. Am J Ment Defic 90: 490-500.
Dupont A, Vaeth M, Videbech P. 1986. Mortality and life expectancy of Down's syndrome in Denmark. J Ment Defic Res 30: 111-120.
Smink M, Eerdmans-Dubbelt SLC, van der Wouden JC. 1992. Medische problemen van verstandelijk gehandicapten in een gezinsvervangend tehuis. Huisarts Wet 35: 461-464.
Schneider MJ, Loots GMP, Reuter J. 1990. Kent Infant Development Scale (KID-N). Nederlandse uitgave. Lisse: Swets & Zeitlinger.
Moss SC. 1991. Age and functional abilities of people with a mental handicap: evidence from the Wessex mental handicap register. J Ment Defic Res 35: 430-445.
Caputo AR, Wagner RS, Reynolds DR, Guo S, Goel AK. 1989. Down syndrome: clinical review of ocular features. Clin Pediatr 28: 355-358.
Gardiner PA. 1967. Visual defects in cases of Down's syndrome and in other mentally handicapped children. Br J Ophthalmol 51: 469-474.
Jones KL. 1997. Smith's recognizable patterns of human malformation, 5th ed. Philadelphia: WB Saunders. p 8-13.
Evenhuis HM. 1990. The natural history of dementia in Down's syndrome. Arch Neurol 47: 263-267.
Evenhuis HM. 1995a. Medical aspects of ageing in a population with intellectual disability. I. Visual impairment. J Intellect Disabil Res 39: 19-25.
Evers-Kiebooms G, Vlietinck, R, Fryns, JP, Van den Berghe, H. 1982. Diverse parameters bij het syndroom van Down (mongolisme) en andere trisomieën in België. CBGS Rapport 50: 8.
Shapiro MB, France TD. 1985. The ocular features of Down's syndrome. Am J Ophtalmol 99: 659-663.
Evenhuis HM. 1995b. Medical aspects of ageing in a population with intellectual disability. II. Hearing impairment. J Intellect Disabil Res 39: 27-33.
Friedman DL, Kastner T, Pond WS, Rice O'Brien D. 1989. Thyroid dysfunction in individuals with Down syndrome. Arch Intern Med 149: 1990-1993.
Van Buggenhout GJCM, Hamel BCJ, Trommelen JCM, Mieloo H, Smeets DFCM. 1994. Down-Turner syndrome: case report and review. J Med Genet 31: 807-810.
Fryns JP, Kleczkowska A. 1986. Reciprocal translocation mosaicism in man (letter to the editor). Am J Med Genet 25: 175-176.
Kennerley Bankes JL. 1974. Eye defects of mentally handicapped children. Br Med J 2: 533-535.
Walsh SZ. 1981. Keratoconus and blindness in 469 institutionalised subjects with Down syndrome and other causes of mental retardation. J Ment Defic Res 25: 243-251.
Fishier K, Koch R. 1991. Mental development in Down syndrome mosaicism. Am J Ment Retard 96: 345-351.
Norman MG, McGillivray BC, Kalousek DK, Hill A, Poskitt KJ. 1995. Congenital malformations of the brain. Pathologic, embryologic, clinical, radiologic and genetic aspects. New York: Oxford University Press.
Pueschel SM, Annerén G, Durlach R, Flores J, Sustrová, M, Verma, IC. 1995. Committee report. Guidelines for optimal medical care of persons with Down syndrome. Acta Paediatr 84: 823-827.
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1995
1994
1992; 35
1992; 36
1962; 54
1991
1995; 4
1987; 17
1989; 28
1995a.; 39
1995; 84
1990; 27
1993; 97
1986; 25
1965
1988; 66
1982; 157
1989; 14
1992; 62
1981; 56
1994; 7
Hoefnagel (BIB32) 1989
Korenberg (BIB41) 1990; 47
(BIB5) 1994
Evenhuis (BIB19) 1992; 36
Gardiner (BIB30) 1967; 51
Caputo (BIB8) 1989; 28
Eissler (BIB16) 1962; 54
Mattei (BIB43) 1981; 56
Buchanan (BIB7) 1990; 19
Friedman (BIB27) 1989; 149
Walsh (BIB62) 1981; 25
Kelly (BIB37) 1996; 5
Thase (BIB56) 1982; 26
Alembik (BIB2) 1996; 4
Evenhuis (BIB24) 1992; 97
Jacobson (BIB33) 1988; 66
Dahle (BIB12) 1986; 90
Stinissen (BIB55) 1970
Fishler (BIB26) 1991; 96
Van Buggenhout (BIB58) 1994; 31
Fuentes (BIB29) 1995; 4
Evers-Kiebooms (BIB25) 1982; 50
Norman (BIB48) 1995
Moss (BIB46) 1991; 35
Aitchinson (BIB1) 1990; 34
Brown (BIB6) 1989; 14
Dinani (BIB13) 1990; 34
Evenhuis (BIB23) 1991
Katz (BIB36) 1994
Dupont (BIB14) 1986; 30
Stinissen (BIB54) 1965
McGrother (BIB45) 1990; 34
Smink (BIB53) 1992; 35
Verpoorten (BIB61) 1995; 24
Pueschel (BIB50) 1995; 84
Mul (BIB47) 1997; 40
Pueschel (BIB49) 1985; 139
Annerén (BIB3) 1992; 62
Evenhuis (BIB21) 1995b; 39
Trommelen (BIB57) 1994; 2
Kinnell (BIB39) 1987; 17
Warburg (BIB63) 1982; 157
Fryns (BIB28) 1986; 25
Evenhuis (BIB18) 1991; 135
Kleczkowska (BIB40) 1990; 27
Shapiro (BIB52) 1985; 99
Schneider (BIB51) 1990
Van Haasen (BIB60) 1986
Edwards (BIB15) 1972; 9
Jones (BIB35) 1997
Janicki (BIB34) 1986; 90
Crandell (BIB10) 1993; 97
Maurizi (BIB44) 1995; 24
Cullen (BIB11) 1963; 47
Harper (BIB31) 1994
Warren (BIB64) 1989; 155
Evenhuis (BIB20) 1995a; 39
Evenhuis (BIB22) 1996; 140
Van der Meulen (BIB59) 1983
Kraijer (BIB42) 1990
Cooper (BIB9) 1984; 101
(BIB4) 1986; 1
Evenhuis (BIB17) 1990; 47
Kennerley Bankes (BIB38) 1974; 2
References_xml – volume: 50
  issue: 8
  year: 1982
  article-title: Diverse parameters bij het syndroom van Down (mongolisme) en andere trisomieën in België
  publication-title: CBGS Rapport
– start-page: 60
  year: 1994
  end-page: 61
– volume: 4
  start-page: 28
  issue: Suppl 1
  year: 1996
  article-title: Anomalies of thyroid function in Down syndrome children
  publication-title: Eur J Hum Genet
– volume: 66
  start-page: 457
  year: 1988
  end-page: 462
  article-title: Ophthalmology in mentally retarded adults
  publication-title: A clinical survey. Acta Ophthalmol
– volume: 25
  start-page: 243
  year: 1981
  end-page: 251
  article-title: Keratoconus and blindness in 469 institutionalised subjects with Down syndrome and other causes of mental retardation
  publication-title: J Ment Defic Res
– volume: 39
  start-page: 19
  year: 1995a.
  end-page: 25
  article-title: Medical aspects of ageing in a population with intellectual disability. I. Visual impairment
  publication-title: J Intellect Disabil Res
– volume: 28
  start-page: 355
  year: 1989
  end-page: 358
  article-title: Down syndrome: clinical review of ocular features
  publication-title: Clin Pediatr
– volume: 149
  start-page: 1990
  year: 1989
  end-page: 1993
  article-title: Thyroid dysfunction in individuals with Down syndrome
  publication-title: Arch Intern Med
– volume: 7
  start-page: 29
  issue: 2
  year: 1994
  end-page: 32
  article-title: Prevalentie van slechthorendheid in een geïnstitutionaliseerde populatie verstandelijk gehandicapten zonder Down syndroom
  publication-title: Logopedie
– volume: 5
  start-page: 630
  year: 1996
  end-page: 634
  article-title: Eye examination and vision testing
  publication-title: Br J Nurs
– year: 1990
– volume: 34
  start-page: 41
  year: 1990
  end-page: 48
  article-title: Eye abnormalities in the mentally handicapped
  publication-title: J Ment Defic Res
– year: 1994
– volume: 96
  start-page: 345
  year: 1991
  end-page: 351
  article-title: Mental development in Down syndrome mosaicism
  publication-title: Am J Ment Retard
– volume: 47
  start-page: 236
  year: 1990
  end-page: 246
  article-title: Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype
  publication-title: Am J Hum Genet
– year: 1986
– volume: 101
  start-page: 18
  year: 1984
  end-page: 24
  article-title: L‐thyroxine therapy in subclinical hypothyroidism
  publication-title: Ann Intern Med
– volume: 9
  start-page: 162
  year: 1972
  end-page: 167
  article-title: Ocular findings in develop‐mentally handicapped children
  publication-title: J Pediatr Ophtalmol
– volume: 40
  start-page: 301
  year: 1997
  end-page: 304
  article-title: Slechthorendheid bij mensen met een verstandelijke handicap in de huisartspraktijk
  publication-title: Huisarts Wet
– volume: 135
  start-page: 1581
  year: 1991
  end-page: 1584
  article-title: Veel voorkomende, maar weinig onderkende aandoeningen bij volwassenen met het syndroom van Down
  publication-title: Ned Tijdschr Geneesk
– volume: 39
  start-page: 27
  year: 1995b.
  end-page: 33
  article-title: Medical aspects of ageing in a population with intellectual disability
  publication-title: II. Hearing impairment. J Intellect Disabil Res
– volume: 30
  start-page: 111
  year: 1986
  end-page: 120
  article-title: Mortality and life expectancy of Down's syndrome in Denmark
  publication-title: J Ment Defic Res
– year: 1965
– volume: 35
  start-page: 430
  year: 1991
  end-page: 445
  article-title: Age and functional abilities of people with a mental handicap: evidence from the Wessex mental handicap register
  publication-title: J Ment Defic Res
– start-page: 99
  year: 1989
  end-page: 131
– volume: 51
  start-page: 469
  year: 1967
  end-page: 474
  article-title: Visual defects in cases of Down's syndrome and in other mentally handicapped children
  publication-title: Br J Ophthalmol
– volume: 31
  start-page: 807
  year: 1994
  end-page: 810
  article-title: Down‐Turner syndrome: case report and review
  publication-title: J Med Genet
– volume: 14
  start-page: 241
  year: 1989
  end-page: 246
  article-title: The skull‐base and nasopharynx in Down's syndrome in relation to hearing impairment
  publication-title: Clin Otolaryngol
– volume: 97
  start-page: 47
  year: 1992
  end-page: 56
  article-title: Hearing loss in middle‐age persons with Down syndrome
  publication-title: Am J Ment Retard
– year: 1983
– volume: 97
  start-page: 568
  year: 1993
  end-page: 574
  article-title: Incidence of excessive/impacted cerumen in individuals with mental retardation: a longitudinal investigation
  publication-title: Am J Ment Retard
– start-page: 283
  year: 1994
  end-page: 285
– volume: 25
  start-page: 175
  year: 1986
  end-page: 176
  article-title: Reciprocal translocation mosaicism in man (letter to the editor)
  publication-title: Am J Med Genet
– volume: 26
  start-page: 177
  year: 1982
  end-page: 192
  article-title: Longevity and mortality in Down's syndrome
  publication-title: J Ment Defic Res
– volume: 17
  start-page: 387
  year: 1987
  end-page: 392
  article-title: Thyroid dysfunction in institutionalised Down's syndrome adults
  publication-title: Psychol Med
– volume: 36
  start-page: 337
  year: 1992
  end-page: 347
  article-title: Evaluation of a screening instrument for dementia in ageing mentally retarded persons
  publication-title: J Intellect Disabil Res
– volume: 47
  start-page: 321
  year: 1963
  end-page: 330
  article-title: Mongolism (Down's syndrome) and keratoconus
  publication-title: Br J Ophthalmol
– volume: 155
  start-page: 202
  year: 1989
  end-page: 205
  article-title: Major depression in Down's syndrome
  publication-title: Br J Psychiatry
– volume: 4
  start-page: 1935
  year: 1995
  end-page: 1944
  article-title: A new human gene from the Down syndrome critical region encodes a proline‐rich protein highly expressed in fetal brain and heart
  publication-title: Hum Mol Genet
– volume: 140
  start-page: 1851
  issue: 37
  year: 1996
  end-page: 1854
  article-title: Richtlijnen voor diagnostiek en behandeling van slechthorendheid bij mensen met een verstandelijke handicap
  publication-title: Ned Tijdschr Geneesk
– volume: 139
  start-page: 636
  year: 1985
  end-page: 639
  article-title: Thyroid dysfunction in Down syndrome
  publication-title: Am J Dis Child
– volume: 84
  start-page: 823
  year: 1995
  end-page: 827
  article-title: Committee report
  publication-title: Guidelines for optimal medical care of persons with Down syndrome. Acta Paediatr
– volume: 62
  start-page: 628
  year: 1992
  end-page: 631
  article-title: Abnormal serum IgG subclass pattern in children with Down's syndrome
  publication-title: Arch Dis Child
– volume: 19
  start-page: 103
  year: 1990
  end-page: 110
  article-title: Early onset of presbyacusis in Down syndrome
  publication-title: Scand Audiol
– volume: 90
  start-page: 636
  year: 1986
  end-page: 642
  article-title: Hearing and otologic disorders in children with Down syndrome
  publication-title: Am J Ment Defic
– volume: 2
  start-page: 533
  year: 1974
  end-page: 535
  article-title: Eye defects of mentally handicapped children
  publication-title: Br Med J
– volume: 56
  start-page: 409
  year: 1981
  end-page: 411
  article-title: Trisomy 21 for the region 21q223: identification by high‐resolution R‐banding patterns
  publication-title: Hum Genet
– volume: 24
  start-page: 49
  issue: Suppl 41
  year: 1995
  end-page: 50
  article-title: A tactile‐auditory conditioning procedure for the hearing assessment of persons with autism and mental retardation
  publication-title: Scand Audiol
– volume: 1
  start-page: 251
  year: 1986
  end-page: 252
  article-title: Subclinical hypothyroidism (editorial)
  publication-title: Lancet
– volume: 47
  start-page: 263
  year: 1990
  end-page: 267
  article-title: The natural history of dementia in Down's syndrome
  publication-title: Arch Neurol
– volume: 90
  start-page: 490
  year: 1986
  end-page: 500
  article-title: General trends in sensory, physical, and behavioral abilities among older mentally retarded persons
  publication-title: Am J Ment Defic
– start-page: 8
  year: 1997
  end-page: 13
– volume: 24
  start-page: 5
  issue: Suppl 41
  year: 1995
  end-page: 7
  article-title: Objective methods of hearing assessment: an introduction
  publication-title: Scand Audiol
– year: 1995
– volume: 27
  start-page: 505
  year: 1990
  end-page: 507
  article-title: On the variable effect of mosaic normal/balanced chromosomal rearrangements in man
  publication-title: J Med Genet
– year: 1970
– volume: 35
  start-page: 461
  year: 1992
  end-page: 464
  article-title: Medische problemen van verstandelijk gehandicapten in een gezinsvervangend tehuis
  publication-title: Huisarts Wet
– volume: 99
  start-page: 659
  year: 1985
  end-page: 663
  article-title: The ocular features of Down's syndrome
  publication-title: Am J Ophtalmol
– year: 1991
– volume: 34
  start-page: 49
  year: 1990
  end-page: 57
  article-title: Recent trends in incidence, morbidity and survival in Down's syndrome
  publication-title: J Ment Defic Res
– volume: 157
  start-page: 72
  year: 1982
  end-page: 81
  article-title: Why are the blind and severely visually impaired children with mental retardation much more retarded than the sighted children
  publication-title: Acta Ophthalmol Suppl
– volume: 34
  start-page: 187
  year: 1990
  end-page: 193
  article-title: Down's syndrome and thyroid disorder
  publication-title: J Ment Defic Res
– volume: 54
  start-page: 398
  year: 1962
  end-page: 406
  article-title: The common eye findings in mongolism
  publication-title: Am J Ophthalmol
– volume: 140
  start-page: 1851
  year: 1996
  ident: BIB22
  publication-title: Ned Tijdschr Geneesk
  contributor:
    fullname: Evenhuis
– volume: 97
  start-page: 568
  year: 1993
  ident: BIB10
  publication-title: Am J Ment Retard
  contributor:
    fullname: Crandell
– volume: 26
  start-page: 177
  year: 1982
  ident: BIB56
  publication-title: J Ment Defic Res
  contributor:
    fullname: Thase
– volume: 90
  start-page: 490
  year: 1986
  ident: BIB34
  publication-title: Am J Ment Defic
  contributor:
    fullname: Janicki
– volume: 34
  start-page: 49
  year: 1990
  ident: BIB45
  publication-title: J Ment Defic Res
  contributor:
    fullname: McGrother
– volume: 35
  start-page: 430
  year: 1991
  ident: BIB46
  publication-title: J Ment Defic Res
  contributor:
    fullname: Moss
– volume: 34
  start-page: 41
  year: 1990
  ident: BIB1
  publication-title: J Ment Defic Res
  contributor:
    fullname: Aitchinson
– volume-title: Diagnostic and statistical manual of mental disorders
  year: 1994
  ident: BIB5
– volume: 14
  start-page: 241
  year: 1989
  ident: BIB6
  publication-title: Clin Otolaryngol
  doi: 10.1111/j.1365-2273.1989.tb00368.x
  contributor:
    fullname: Brown
– volume: 39
  start-page: 27
  year: 1995b
  ident: BIB21
  publication-title: J Intellect Disabil Res
  doi: 10.1111/j.1365-2788.1995.tb00910.x
  contributor:
    fullname: Evenhuis
– volume: 25
  start-page: 243
  year: 1981
  ident: BIB62
  publication-title: J Ment Defic Res
  contributor:
    fullname: Walsh
– volume-title: Pathologic, embryologic, clinical, radiologic and genetic aspects
  year: 1995
  ident: BIB48
  contributor:
    fullname: Norman
– volume-title: Wechsler intelligence scale for children-revised, Nederlandse uitgave
  year: 1986
  ident: BIB60
  contributor:
    fullname: Van Haasen
– volume: 56
  start-page: 409
  year: 1981
  ident: BIB43
  publication-title: Hum Genet
  doi: 10.1007/BF00274703
  contributor:
    fullname: Mattei
– volume: 31
  start-page: 807
  year: 1994
  ident: BIB58
  publication-title: J Med Genet
  doi: 10.1136/jmg.31.10.807
  contributor:
    fullname: Van Buggenhout
– volume: 51
  start-page: 469
  year: 1967
  ident: BIB30
  publication-title: Br J Ophthalmol
  doi: 10.1136/bjo.51.7.469
  contributor:
    fullname: Gardiner
– volume: 27
  start-page: 505
  year: 1990
  ident: BIB40
  publication-title: J Med Genet
  doi: 10.1136/jmg.27.8.505
  contributor:
    fullname: Kleczkowska
– volume: 90
  start-page: 636
  year: 1986
  ident: BIB12
  publication-title: Am J Ment Defic
  contributor:
    fullname: Dahle
– volume: 40
  start-page: 301
  year: 1997
  ident: BIB47
  publication-title: Huisarts Wet
  contributor:
    fullname: Mul
– volume: 19
  start-page: 103
  year: 1990
  ident: BIB7
  publication-title: Scand Audiol
  doi: 10.3109/01050399009070760
  contributor:
    fullname: Buchanan
– volume: 39
  start-page: 19
  year: 1995a
  ident: BIB20
  publication-title: J Intellect Disabil Res
  doi: 10.1111/j.1365-2788.1995.tb00909.x
  contributor:
    fullname: Evenhuis
– volume: 99
  start-page: 659
  year: 1985
  ident: BIB52
  publication-title: Am J Ophtalmol
  doi: 10.1016/S0002-9394(14)76031-3
  contributor:
    fullname: Shapiro
– start-page: 8
  volume-title: Smith's recognizable patterns of human malformation
  year: 1997
  ident: BIB35
  contributor:
    fullname: Jones
– start-page: 60
  volume-title: Practical genetic counseling
  year: 1994
  ident: BIB31
  contributor:
    fullname: Harper
– volume: 54
  start-page: 398
  year: 1962
  ident: BIB16
  publication-title: Am J Ophthalmol
  doi: 10.1016/0002-9394(62)93757-1
  contributor:
    fullname: Eissler
– volume-title: Handleiding bij de Nederlandse aanpassing
  year: 1970
  ident: BIB55
  contributor:
    fullname: Stinissen
– volume: 24
  start-page: 49
  year: 1995
  ident: BIB61
  publication-title: Scand Audiol
  contributor:
    fullname: Verpoorten
– volume: 34
  start-page: 187
  year: 1990
  ident: BIB13
  publication-title: J Ment Defic Res
  contributor:
    fullname: Dinani
– volume: 135
  start-page: 1581
  year: 1991
  ident: BIB18
  publication-title: Ned Tijdschr Geneesk
  contributor:
    fullname: Evenhuis
– volume: 47
  start-page: 236
  year: 1990
  ident: BIB41
  publication-title: Am J Hum Genet
  contributor:
    fullname: Korenberg
– volume: 139
  start-page: 636
  year: 1985
  ident: BIB49
  publication-title: Am J Dis Child
  contributor:
    fullname: Pueschel
– start-page: 99
  volume-title: Mentale retardatie vanuit psychologische optiek
  year: 1989
  ident: BIB32
  contributor:
    fullname: Hoefnagel
– volume: 157
  start-page: 72
  year: 1982
  ident: BIB63
  publication-title: Acta Ophthalmol Suppl
  contributor:
    fullname: Warburg
– volume: 1
  start-page: 251
  year: 1986
  ident: BIB4
  publication-title: Lancet
– volume-title: Dementie vragenlijst voor zwakzinnigen (DVZ)
  year: 1991
  ident: BIB23
  contributor:
    fullname: Evenhuis
– volume: 84
  start-page: 823
  year: 1995
  ident: BIB50
  publication-title: Acta Paediatr
  doi: 10.1111/j.1651-2227.1995.tb13768.x
  contributor:
    fullname: Pueschel
– volume-title: Nederlandse Uitgave (BOS 2-30)
  year: 1983
  ident: BIB59
  contributor:
    fullname: Van der Meulen
– volume: 97
  start-page: 47
  year: 1992
  ident: BIB24
  publication-title: Am J Ment Retard
  contributor:
    fullname: Evenhuis
– volume: 5
  start-page: 630
  year: 1996
  ident: BIB37
  publication-title: Br J Nurs
  doi: 10.12968/bjon.1996.5.10.630
  contributor:
    fullname: Kelly
– volume: 66
  start-page: 457
  year: 1988
  ident: BIB33
  publication-title: Acta Ophthalmol
  doi: 10.1111/j.1755-3768.1988.tb04040.x
  contributor:
    fullname: Jacobson
– volume: 149
  start-page: 1990
  year: 1989
  ident: BIB27
  publication-title: Arch Intern Med
  doi: 10.1001/archinte.1989.00390090058012
  contributor:
    fullname: Friedman
– volume: 155
  start-page: 202
  year: 1989
  ident: BIB64
  publication-title: Br J Psychiatry
  doi: 10.1192/bjp.155.2.202
  contributor:
    fullname: Warren
– volume: 50
  start-page: 8
  year: 1982
  ident: BIB25
  publication-title: CBGS Rapport
  contributor:
    fullname: Evers-Kiebooms
– volume: 4
  start-page: 28
  year: 1996
  ident: BIB2
  publication-title: Eur J Hum Genet
  contributor:
    fullname: Alembik
– volume: 101
  start-page: 18
  year: 1984
  ident: BIB9
  publication-title: Ann Intern Med
  doi: 10.7326/0003-4819-101-1-18
  contributor:
    fullname: Cooper
– volume: 25
  start-page: 175
  year: 1986
  ident: BIB28
  publication-title: Am J Med Genet
  doi: 10.1002/ajmg.1320250124
  contributor:
    fullname: Fryns
– year: 1965
  ident: BIB54
  contributor:
    fullname: Stinissen
– volume: 47
  start-page: 321
  year: 1963
  ident: BIB11
  publication-title: Br J Ophthalmol
  doi: 10.1136/bjo.47.6.321
  contributor:
    fullname: Cullen
– start-page: 283
  volume-title: Handbook of clinical audiology
  year: 1994
  ident: BIB36
  contributor:
    fullname: Katz
– volume: 17
  start-page: 387
  year: 1987
  ident: BIB39
  publication-title: Psychol Med
  doi: 10.1017/S0033291700024946
  contributor:
    fullname: Kinnell
– volume: 4
  start-page: 1935
  year: 1995
  ident: BIB29
  publication-title: Hum Mol Genet
  doi: 10.1093/hmg/4.10.1935
  contributor:
    fullname: Fuentes
– volume-title: Nederlandse uitgave
  year: 1990
  ident: BIB51
  contributor:
    fullname: Schneider
– volume: 2
  start-page: 533
  year: 1974
  ident: BIB38
  publication-title: Br Med J
  doi: 10.1136/bmj.2.5918.533
  contributor:
    fullname: Kennerley Bankes
– volume: 9
  start-page: 162
  year: 1972
  ident: BIB15
  publication-title: J Pediatr Ophtalmol
  contributor:
    fullname: Edwards
– volume: 96
  start-page: 345
  year: 1991
  ident: BIB26
  publication-title: Am J Ment Retard
  contributor:
    fullname: Fishler
– volume: 35
  start-page: 461
  year: 1992
  ident: BIB53
  publication-title: Huisarts Wet
  contributor:
    fullname: Smink
– volume: 24
  start-page: 5
  year: 1995
  ident: BIB44
  publication-title: Scand Audiol
  contributor:
    fullname: Maurizi
– volume: 62
  start-page: 628
  year: 1992
  ident: BIB3
  publication-title: Arch Dis Child
  doi: 10.1136/adc.67.5.628
  contributor:
    fullname: Annerén
– volume: 28
  start-page: 355
  year: 1989
  ident: BIB8
  publication-title: Clin Pediatr
  doi: 10.1177/000992288902800804
  contributor:
    fullname: Caputo
– volume: 47
  start-page: 263
  year: 1990
  ident: BIB17
  publication-title: Arch Neurol
  doi: 10.1001/archneur.1990.00530030029011
  contributor:
    fullname: Evenhuis
– volume: 2
  start-page: 29
  year: 1994
  ident: BIB57
  publication-title: Logopedie
  contributor:
    fullname: Trommelen
– volume: 30
  start-page: 111
  year: 1986
  ident: BIB14
  publication-title: J Ment Defic Res
  contributor:
    fullname: Dupont
– volume: 36
  start-page: 337
  year: 1992
  ident: BIB19
  publication-title: J Intellect Disabil Res
  doi: 10.1111/j.1365-2788.1992.tb00532.x
  contributor:
    fullname: Evenhuis
– volume-title: Sociale Redzaamheidsschaal
  year: 1990
  ident: BIB42
  contributor:
    fullname: Kraijer
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Snippet Ninety‐six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic...
Ninety-six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic...
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SubjectTerms Adult
Biological and medical sciences
Chromosome aberrations
Cytogenetics
Down syndrome
Down Syndrome - epidemiology
Down Syndrome - genetics
Female
Hearing - physiology
hearing loss
Humans
Intellectual Disability - etiology
Intellectual Disability - pathology
Male
Medical genetics
Medical sciences
mental retardation
Middle Aged
thyroid function
Thyroid Gland - metabolism
trisomy 21
vision loss
Visual Acuity
Title Down syndrome in a population of elderly mentally retarded patients: Genetic-diagnostic survey and implications for medical care
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https://www.ncbi.nlm.nih.gov/pubmed/10398264
https://search.proquest.com/docview/69881712
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